FDA Warning Letter — Wexford Labs Inc

Case 391397 — FEI 1000147951

The FDA took a Warning Letter action against Wexford Labs Inc on January 10, 2013 (Kirkwood, MO). The action was issued by CDRH and concerns devices products. This facility has 3 recent FDA inspections on record.

Action Details

Facility
Wexford Labs Inc
Date
January 10, 2013
Fiscal Year
2013
Product Type
Devices
Center
CDRH
Location
Kirkwood, MO (United States)